Canonical Allele Identifier: PA916023705
Gene: TSC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 571007
ClinVar RCV Id: RCV000692026 RCV002473112
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001305761.1:p.Cys655Gly
CA394273325
NM_001318832.2:c.1963T>G